HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908670Generated: October 30, 2026
HCID 67392406, compound → HCID 44476497, compound
https://huagongshe.com/reaction/908670
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 67392406 | HCID 67392406 | — |
| Reactant | HCID 67392639 | HCID 67392639 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 44476497 | HCID 44476497 | 9% |
Reaction Steps
5-({3-[(3-aminopropyl)(methyl)amino]propyl}amino)-2-methyl-1,3-benzothiazole-4,7-dione is solubilized in 250 ml of ethanol and 2.12 g (6.16 mmol; 0.8 equivalent) of 5-methoxy-N-(4-methoxyphenyl)-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide is added. The reaction mixture is maintained under stirring at 60° C. for 4 hours, then the solvent is evaporated off under reduced pressure. The residue is then purified by chromatography on a silica column (eluent: dichloromethane/methanol: 95/5) and 450 mg (yield=9%) of N-(4-methoxyphenyl)-5-{[3-(methyl{3-[(2-methyl-4,7-dioxo-4,7-dihydro-1,3-benzothiazol-5-yl)amino]propyl}amino)propyl]amino}-4,7-dioxo-4,7-dihydro-1,3-benzothiazole-2-carboxamide is obtained in the form of red powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017637B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-2fbccc395f3a4f5a8bd725df1048cb9b |
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| Source note | uspto-grants-2011_09 |
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